Canon USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Canon USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DIGITAL RADIOGRAPHY CXDI-40G COMPACT, PACS SOFTWARE SOLUTION 2003, CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
48
Total
48
Cleared
0
Denied
Canon USA, Inc. has 48 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 48 cleared submissions from 1984 to 2009. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Canon USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Canon USA, Inc.
48 devices
Cleared
Mar 24, 2009
DIGITAL RADIOGRAPHY CXDI-40G COMPACT
Radiology
15d
Cleared
Dec 15, 2003
PACS SOFTWARE SOLUTION 2003
Radiology
27d
Cleared
Jun 11, 2003
CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
Radiology
15d
Cleared
Jun 06, 2003
CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
Ophthalmic
10d
Cleared
Nov 22, 2002
CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G
Radiology
14d
Cleared
Nov 05, 2002
DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS
Radiology
11d
Cleared
Jan 02, 2002
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31
Radiology
398d
Cleared
Jun 21, 2000
CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100
Ophthalmic
323d
Cleared
Oct 13, 1999
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22
Radiology
75d
Cleared
Nov 04, 1998
CANON X-RAY DIGITAL CAMERA CXDI-11
Radiology
187d
Cleared
May 06, 1998
NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM
Ophthalmic
103d
Cleared
Mar 03, 1997
CANON TX-10 TONOMETER
Ophthalmic
208d
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